Discovery of LAH-1 as potent c-Met inhibitor for the treatment of non-small cell lung cancer

J Enzyme Inhib Med Chem. 2024 Dec;39(1):2286435. doi: 10.1080/14756366.2023.2286435. Epub 2023 Dec 11.

Abstract

ABSTRCTDysregulated HGF/c-Met pathway has been implicated in multiple human cancers and has become an attractive target for cancer intervention. Herein, we report the discovery of N-(3-fluoro-4-((2-(3-hydroxyazetidine-1-carboxamido)pyridin-4-yl)oxy)phenyl)-1-(4-fluorophenyl)-4-methyl-6-oxo-1,6-dihydropyridazine-3-carboxamide (LAH-1), which demonstrated nanomolar MET kinase activity as well as desirable antiproliferative activity, especially against EBC-1 cells. Mechanism studies confirmed the effects of LAH-1 on modulation of HGF/c-Met pathway, induction of cell apoptosis, inhibition on colony formation as well as cell migration and invasion. In addition, LAH-1 also showed desirable in vitro ADME properties as well as acceptable in vivo PK parameters. The design, synthesis, and characterisation of LAH-1 are described herein.

Keywords: LAH-1; NSCLC; antitumor activity; c-Met.

MeSH terms

  • Carcinoma, Non-Small-Cell Lung* / drug therapy
  • Cell Line, Tumor
  • Cell Proliferation
  • Humans
  • Lung Neoplasms* / drug therapy
  • Protein Kinase Inhibitors / pharmacology
  • Proto-Oncogene Proteins c-met

Substances

  • Proto-Oncogene Proteins c-met
  • Protein Kinase Inhibitors